Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: MYH10[original query] |
---|
De novo mutations in moderate or severe intellectual disability. PLoS genetics 2014 Oct 10 (10): e1004772. Hamdan Fadi F, Srour Myriam, Capo-Chichi Jose-Mario, Daoud Hussein, Nassif Christina, Patry Lysanne, Massicotte Christine, Ambalavanan Amirthagowri, Spiegelman Dan, Diallo Ousmane, Henrion Edouard, Dionne-Laporte Alexandre, Fougerat Anne, Pshezhetsky Alexey V, Venkateswaran Sunita, Rouleau Guy A, Michaud Jacques |
The Contribution of Mosaic Variants to Autism Spectrum Disorder. PLoS genetics 2016 Sep 12 (9): e1006245. Freed Donald, Pevsner Jonath |
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness. Molecular neuropsychiatry 2015 Oct 1 (3): 175-190. Johnstone Mandy, Maclean Alan, Heyrman Lien, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, De Rijk Peter, Goossens Dirk, Adolfsson Rolf, St Clair David M, Hall Jeremy, Lawrie Stephen M, McIntosh Andrew M, Del-Favero Jurgen, Blackwood Douglas H R, Pickard Benjamin |
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip. Molecular genetics and genomics : MGG 2022 12 298 (2): 329-342. Dembic Maja, van Brakel Andersen Lars, Larsen Martin Jakob, Mechlenburg Inger, Søballe Kjeld, Hertz Jens Micha |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: